「EVI1 and GATA2 misexpression induced by inv(3)(q21q26) contribute to megakaryocyte-lineage skewing and leukemogenesis.」の関連論文
-
Two effects of GATA2 enhancer repositioning by 3q chromosomal rearrangements.
-
Aberrant EVI1 splicing contributes to EVI1-rearranged leukemia
-
RUNX1 rearrangement in mature B-cell acute lymphoblastic leukemia with non-L3 morphology
-
Cryptic insertion of CBFB into MYH11 leading to a type D fusion in acute myeloid leukemia with normal karyotype
-
Unexpected appearance of KMT2A::MLLT10 fusion transcript in acute myeloid leukemia with t(5;11)(q31;q23.3)
-
Down syndrome-related transient abnormal myelopoiesis is attributed to a specific erythro-megakaryocytic subpopulation with GATA1 mutation
-
Protective role of residual Tet2/Tet3 alleles in development of myeloid leukemia
-
Integrated Genomic Analysis Identifies UBTF Tandem Duplications as a Recurrent Lesion in Pediatric Acute Myeloid Leukemia
-
Amplified EPOR/JAK2 Genes Define a Unique Subtype of Acute Erythroid Leukemia
-
PML-RARαはMED1との結合を介して全トランス型レチノイン酸依存性の転写活性化を誘導する
-
A RUNX-targeted gene switch-off approach modulates the BIRC5/PIF1-p21 pathway and reduces glioblastoma growth in mice
-
Analysis of disease model iPSCs derived from patients with a novel Fanconi anemia-like IBMFS ADH5/ALDH2 deficiency
-
Biclonal Diffuse Large B-cell Lymphoma Commonly Characterized by Partial Trisomy 18q Involving MALT1 and BCL2
-
成獣ライディッヒ細胞における性染色体の機能解析
-
HER2 G776S mutation promotes oncogenic potential in colorectal cancer cells when accompanied by loss of APC function
-
Sequencing of selected chromatin remodelling genes reveals increased burden of rare missense variants in ASD patients from the Japanese population
-
Dissecting the Intracellular Molecular Mechanisms to Address Pathogenesis of Multifactorial Diseases
-
Pluripotent stem cell model of Shwachman-Diamond syndrome reveals apoptotic predisposition of hemoangiogenic progenitors
-
DNA methyltransferase 3B plays a protective role against hepatocarcinogenesis caused by chronic inflammation via maintaining mitochondrial homeostasis
-
Functional Analysis of Cancer-associated IDH mutations
-
Identification of T cell receptors targeting a neoantigen derived from recurrently mutated FGFR3
-
Two mouse models carrying truncating mutations in Magel2 show distinct phenotypes
-
Rescue of recurrent deep intronic mutation underlying cell type-dependent quantitative NEMO deficiency
-
HBO1-MLL interaction promotes AF4/ENL/P-TEFb-mediated leukemogenesis
-
Prognostic stratification for IDH-wild-type lower-grade astrocytoma by Sanger sequencing and copy-number alteration analysis with MLPA
-
Functional analysis of P53 negative regulators in Bombyx mori
-
Inherent genomic properties underlie the epigenomic heterogeneity of human induced pluripotent stem cells
-
The EZH2 inhibitor tazemetostat upregulates the expression of CCL17/TARC in B-cell lymphoma and enhances T-cell recruitment
-
De Novo T790M Mutation in an L858R Epidermal Growth Factor Receptor Mutant-Associated Lung Adenocarcinoma
-
Azacitidine is a potential therapeutic drug for pyridoxine-refractory female X-linked sideroblastic anemia
-
Tfl deletion induces extraordinary Cxcl13 secretion and cachexia in VavP-Bcl2 transgenic mice
-
Next Generation Sequencing-Based Transcriptome Predicts Bevacizumab Efficacy in Combination with Temozolomide in Glioblastoma
-
An experience in prenatal diagnosis via QF-PCR of a female child with a 9.9 Mb pure deletion at 18p11.32–11.22
-
Increased CaV1.2 late current by a CACNA1C p.R412M variant causes an atypical Timothy syndrome without syndactyly
-
Compromised anti-tumor–immune features of myeloid cell components in chronic myeloid leukemia patients
-
Stability and Oligomerization of Mutated SMN Protein Determine Clinical Severity of Spinal Muscular Atrophy
-
BRCA1 haploinsufficiency promotes chromosomal amplification under Fenton reaction-based carcinogenesis through ferroptosis-resistance
-
Smooth muscle protein 22α‐Cre recombination in resting cardiac fibroblasts and hematopoietic precursors
-
A mutation in DOK7 in congenital myasthenic syndrome forms aggresome in cultured cells, and reduces DOK7 expression and MuSK phosphorylation in patient-derived iPS cells
-
Myelin protein zero (P0)- and Wnt1-Cre marked muscle resident neural crest-derived mesenchymal progenitor cells give rise to heterotopic ossification in mouse models
-
Setd1a plays pivotal roles for the survival and proliferation of retinal progenitors via histone modifications of Uhrf1
-
Identification of distinct loci for de novo DNA methylation by DNMT3A and DNMT3B during mammalian development
-
Amplified EPOR/JAK2 Genes Define a Unique Subtype of Acute Erythroid Leukemia
-
Lionheart LincRNA alleviates cardiac systolic dysfunction under pressure overload
-
Combination of tumor necrosis factor-α and epidermal growth factor induces the adrenergic-to-mesenchymal transdifferentiation in SH-SY5Y neuroblastoma cells
-
Lusutrombopag effectively promotes the growth and differentiation of megakaryocytic cells from patients with myelodysplastic syndrome
-
Study of the Effects of Inhibition of Epigenetic Regulators on the Proliferation of Hematological Malignant Tumor Cells
-
Identification of novel mutations and reassignment of archival xeroderma pigmentosum group C cell strains from Japanese patients
-
MYCL promotes iPSC-like colony formation via MYC Box 0 and 2 domains
-
Ebf3⁺ niche-derived CXCL12 is required for the localization and maintenance of hematopoietic stem cells